User:MartinGala/zona de pruebas/queries

WikiProject:Medicine

Búsqueda de elementos (Q) en la "lista de interesantes para el proyecto" pero que carecen de etiqueta (Label) / Descripción y Alias en español
Para ejecutar la consulta en WikiData seguir los enlaces:

En WD-Query Service → Run WDQueryService
En Tabernacle → Lanzar consulta en Tabernacle

Código de la consulta

#Wikiproyecto:Medicina
SELECT DISTINCT ?item ?itemLabel WHERE {
  SERVICE wikibase:label { bd:serviceParam wikibase:language "[AUTO_LANGUAGE]". }
  {
    SELECT DISTINCT ?item WHERE {
      ?item p:P5008 ?statement0.
      ?statement0 (ps:P5008/(wdt:P279*)) wd:Q4099686.
    }
    LIMIT 100
    }
  }
ORDER BY ASC (?itemLabel)

Resultados de la consulta anterior ejecutados por Listeria (bot)

Manually update list

This list is periodically updated by a bot. Manual changes to the list will be removed on the next update!

SELECT DISTINCT ?item ?itemLabel WHERE {   SERVICE wikibase:label { bd:serviceParam wikibase:language "[AUTO_LANGUAGE]". }   {     SELECT DISTINCT ?item WHERE {       ?item p:P5008 ?statement0.       ?statement0 (ps:P5008/(wdt:P279*)) wd:Q4099686.     }     LIMIT 100   } } ORDER BY ASC (?itemLabel)

Article	description	Place	start time	end time	coordinate location	image
Acanthamoeba keratitis	Human disease
Barth syndrome	lipid metabolism disorder that has material basis in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin
Brown-Séquard syndrome	human disease
CADASIL	autosomal dominant cerebrovascular disorder characterized by recurrent subcortical ischemic stroke and cognitive impairment
CHARGE syndrome	syndrome that is characterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina
Crigler-Najjar syndrome	bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT)
Dravet syndrome	epilepsy characterized by frequent febrile seizures and with onset before 1 year
Fanconi syndrome	renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting
Felty's syndrome	syndrome that results in rheumatoid arthritis, splenomegaly and neutropenia
Friedreich ataxia	Human disease
Froelich syndrome	hypothalamic disease that is characterized by endocrine dysfunction of the hypothalamic gland resulting in delayed puberty, small testes, and obesity
HAM	human disease
Kabuki syndrome	rare disease
Lennox-Gastaut sindrome	rare but severe childhood-onset epilepsy
Naxos disease	Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma
Pfeiffer syndrome	acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull
Porcine enzootic pneumonia	swine disease
Raynaud disease	Human disease
Rothmund-Thomson syndrome	human disease
Sandhoff disease	lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
Tangier disease	extremely rare inherited human disorder
Waardenburg's syndrome	genetic condition involving hearing loss and depigmentation
adrenocortical carcinoma	adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has material basis in abnormally proliferating cells derives from epithelial cells
akinetopsia	agnosia that is a loss of motion perception
argininemia	urea cycle disorder that involves arginase deficiency resulting in elevated levels of plasma arginine
bacillary angiomatosis	human disease
blepharophimosis	Human disease
blepharospasm	focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks
brachydactyly	bone development disease characterized by short fingers and toes
calcific tendinitis	disorder characterized by deposits of hydroxyapatite (a crystalline calcium phosphate) in any tendon of the body
calciphylaxis	Human disease
cheilitis	inflammation of the lips
choroid plexus carcinoma	choroid plexus cancer that has material basis in epithelial cells of the choroid plexus
chronic inflammatory demyelinating polyradiculoneuropathy	acquired immune-mediated inflammatory disorder of the peripheral nervous system
chronic lymphocytic leukemia	lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood
collagen disease	group of diseases affecting connective tissue
complex regional pain syndrome	array of painful conditions in humans
congenital central hypoventilation syndrome	Human disease
conversion disorder	physical illness or symptoms caused by serious emotional stress
cryptococcosis	potentially fatal disease
dental fluorosis	human disease
diphyllobothriasis	helminthiasis
duodenum cancer	small intestine cancer that is located in the beginning section of the small intestine
dysostosis	bone development disease that results in defective ossification of located in bone
dystonia	human disease
empty sella syndrome	endocrine disease
endometritis	inflammation of inner lining of uterus
ependymoblastoma	Human disease
epidermodysplasia verruciformis	Human disease
filariasis	parasitic disease caused by a family of nematode worms
focal segmental glomerulosclerosis	kidney disease
folie à deux	shared psychosis, a psychiatric syndrome in which symptoms of a delusional belief are transmitted from one individual to another
galactosialidosis	rare disease
glycogen storage disease IV	human disease
granuloma inguinale	sexually transmitted bacterial disease
halo nevus	human disease
heart conduction disease	cardiovascular system disease that involves the heart's electrical conduction system
heart valve disease	disease in the valves of the heart
hemolytic anemia	form of anemia due to hemolysis
hepatocellular adenoma	Hepatocellular adenoma (HA) is a rare benign tumor of the liver
hypercholesterolemia	high levels of cholesterol in the blood
hypochondroplasia	osteochondrodysplasia that has material basis in mutation in the FGFR3 gene which affects ossification of cartilage and results in short limb dwarfism
insulinoma	tumor that produces too much insulin
jaw-winking syndrome	autosomal dominant condition with incomplete penetrance, in which nursing infants will have rhythmic upward jerking of their upper eyelid
lichen planus	chronic disease of skin, tongue or oral mucosa
lipid metabolism disorder	abnormal levels of cholesterol & lipids
melorheostosis	osteosclerosis that has material basis in a mutation of the LEMD3 gene which results in a hyperdense bony cortex
multiple acyl-CoA dehydrogenase deficiency	medical condition
myofascial pain syndrome	human disease
myxomatosis	rabbit disease
noma	Gangrenous infection of the mouth and face
ochronosis	syndrome caused by the accumulation of homogentisic acid in connective tissues
osteitis fibrosa cystica	bone resorption disease that has material basis in hyperparathyroidism which results in hyperactivity in osteoclasts, deformity, and loss of mass located in bone
osteomalacia	bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone
panhypopituitarism	human disease
papilledema	human disease
petrositis	osteomyelitis that has material basis in infection located in petrous part of temporal bone
phosphofructokinase deficiency	Human disease
pinealoma	tumor in endocrine gland located in the pineal gland located in the brain
pityriasis rubra pilaris	Human disease
primary biliary cholangitis	liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts
pseudohypoparathyroidism	human disease
pulmonary hemosiderosis	human disease
purpura	hemorrhagic lesion of the skin caused by bleeding underneath the skin
pyoderma gangrenosum	condition that causes tissue to become necrotic, causing deep ulcers that usually occur on the legs
renal osteodystrophy	Human disease
retrograde amnesia	loss of memory of events that in occurred before the onset of amnesiac condition
sparganosis	Helminthiasis
syndactyly	synostosis that results in the fusion of two or more digits
syndrome of Inappropriate antidiuretic hormone secretion	endocrine disease
thrombophilia	abnormality of blood coagulation that increases the risk of thrombosis (blood clots in blood vessels)
tic disorder	range of neurodevelopmental conditions with motor or phonic spasms
tinea corporis	fungal infection
tinea cruris	type of fungal infection of the groin region in either sex, though more often seen in males
toxic shock syndrome	condition caused by bacterial toxins
tracheitis	inflammation of the trachea
twin-to-twin transfusion syndrome	complication of disproportionate blood supply, resulting in high morbidity and mortality
urethral stricture	narrowing of the urethra caused by injury, instrumentation, infection and certain non-infectious forms of urethritis
uterine cancer	female reproductive organ cancer that is located in the uterus
vulvovaginal candidiasis	excessive growth of yeast in the vagina that results in irritation